Synthesis of 9-substituted tetrahydrodiazepinopurines: Studies toward the total synthesis of asmarines
- Author
- PAPPO, Doron1 ; SHIMONY, Shiri1 ; KASHMAN, Yoel1
[1] School of Chemistry, Tel-Aviv University, Ramat Aviv 69978, Israel - Source
Journal of organic chemistry. 2005, Vol 70, Num 1, pp 199-206, 8 p ; ref : 22 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité biologique Alcaloïde Azote 15 Carbone 13 Composé tricyclique Cyclisation Cytotoxicité Hétérocycle azote Origine végétale Réaction catalytique Spectrométrie RMN Synthèse totale 1,4-Diazépino[1,2,3-g,h]purine dérivé Asmarine B
- Keyword (en)
- Biological activity Alkaloid Nitrogen 15 Carbon 13 Tricyclic compound Cyclization Cytotoxicity Nitrogen heterocycle Plant origin Catalytic reaction NMR spectrometry Total synthesis
- Keyword (es)
- Actividad biológica Alcaloide Compuesto tricíclico Ciclización Citotoxicidad Heterociclo nitrógeno Origen vegetal Reacción catalítica Espectrometría RMN Síntesis total
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16440107
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/jo048622g 
https://dx.doi.org/10.1021/jo048622g
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